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Clinical Trials in Germany / NCT07731490
Recruiting Not applicable

Early Detection and IntervenTion in Heart Failure

NCT07731490 · tracked via the Priya Life Science Germany tracker
Phase
Not applicable
Started
2025-12-03
Last updated
2026-07-28

Condition(s) studied

Heart Failure (HF)

Investigational drug(s) / intervention(s)

Intervention bundle comprising increased awareness, early diagnostics, and early treatment to improve HF prognosis.

Intervention bundle comprising increased awareness, early diagnostics, and early treatment to improve HF prognosis.: The study aims to fill critical gaps and evaluate patient-centred outcomes, including hospitalization for acute HF, and health economic implications by using routine clinical data and the standard operating procedures as part of routine clinical practice in the participating sites.

Study summary

Heart failure (HF) occurs when the heart is no longer able to pump blood effectively throughout the body. This leads to symptoms that gradually worsen over time and are often mistaken for normal signs of aging. Because of its insidious onset, early detection is challenging. Both patients and healthcare professionals are often insufficiently aware of the early signs and symptoms of HF, resulting in delayed diagnosis. Consequently, timely initiation of treatments that could slow disease progression, improve quality of life, and reduce hospitalizations is often missed. Although a simple blood test measuring NT-proBNP levels can facilitate the early diagnosis of HF, it is not routinely used in clinical practice.

The aim of this study is to evaluate whether a combined strategy for the early diagnosis and treatment of HF can reduce hospitalizations. This strategy includes:

1. increasing awareness of HF among patients and physicians,
2. using NT-proBNP testing for the early detection of HF in high-risk patients, and
3. promptly initiating guideline-directed HF treatment when the diagnosis is confirmed.

The researchers will assess whether this strategy effectively reduces hospitalizations due to acute heart failure over an 18-month follow-up period.

Eligibility

Sex
ALL
Min age
65 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * General consent (GC) has not been rejected. * Age ≥ 65 years. * Elective percutaneous coronary intervention\* (PCI), pulmonary vein isolation\* (PVI), pacemaker implantation\* (PM, no cardiac resynchronisation), transcatheter aortic valve intervention\* (TAVI), major non-cardiac surgery\* or presenting with tachyarrhythmia to the emergency department (ED) (without a diagnosis of HF within 24h). * Exclusion criteria are assessed on day 1 after the procedure Exclusion Criteria: * Systolic blood pressure ≤ 95 mmHg * Estimated glomerular filtration rate (GFR) \<30 mL/min/1.73 m2. * Dementia documented in the medical history. * Metastatic cancer in the medical history. * Previously enrolled in this study. * Known HF. * Known allergies, hypersensitivity, or intolerance to SGLT2 Inhibitors / Loop Diuretics / MRA or is excipients. * Non-resident in the country of the recruiting site * Incapacity of the patient to make judgements * Patients not hospitalized overnight * Patients requiring intensive care unit (ICU) or intermediate care (IMC) stay beyond 11:00 a.m. on the first postoperative day or any post-interventional stroke unit stay until 8:00 a.m. on the first postoperative day. * Patients died prior to postinterventional day 1 (8:00 a.m.) * Severe aortic or mitral stenosis

Primary outcome measure(s)

Trial sites (21)

FacilityCityRegionStatus
Universitätsklinik für Innere Medizin II Vienna Austria Not Yet Recruiting
Queen Giovanna University Hospital Sofia Bulgaria Not Yet Recruiting
University Hospital Freiburg-Bad Krozingen Freiburg im Breisgau Germany Not Yet Recruiting
Universitätsklinikum der Ruhr-Universität Bochum Herne Germany Not Yet Recruiting
Herzzentrum Leipzig, Klinik für Innere Medizin/Kardiologie Leipzig Germany Not Yet Recruiting
University Hospital Pisa Pisa Italy Not Yet Recruiting
Erasmus MC Rotterdam Rotterdam Netherlands Not Yet Recruiting
Konkuk University Medical Center Seoul South Korea Recruiting
University Hospital Ramón y Cajal Madrid Madrid Spain Not Yet Recruiting
University Hospital Basel Basel Basel Recruiting
University Hospital Lausanne Lausanne Lausanne Not Yet Recruiting
KSA Kantonsspital Aarau Aarau Switzerland Not Yet Recruiting
Cantonal Hospital Baden Baden Switzerland Not Yet Recruiting
St. Claraspital AG Basel Switzerland Not Yet Recruiting
University Hospital Genève Geneva Switzerland Not Yet Recruiting
Kantonsspital Luzern Lucerne Switzerland Not Yet Recruiting
Hospital Istituto Cardiocentro Ticino Lugano Switzerland Not Yet Recruiting
Kantonsspital St. Gallen Sankt Gallen Switzerland Not Yet Recruiting
Stadtspital Zürich Zurich Switzerland Not Yet Recruiting
University Hospital Zurich Zurich Switzerland Not Yet Recruiting
Royal Infirmary Edinburgh Edinburgh United Kingdom Not Yet Recruiting

More University Hospital, Basel, Switzerland trials in Germany

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07731490 on ClinicalTrials.gov ↗ ← All trials in Germany